Chao Mei
Department of Microbiology and Immunology, College of Medicine, Chang Gung University, 259, Wen-Hwa 1st Road, Kwei-Shan, Tao-yang 333, Taiwan.
Virus Res. 2007 Aug;127(2):208-15. doi: 10.1016/j.virusres.2007.01.003. Epub 2007 Feb 12.
Hepatitis delta virus (HDV) requires the surface antigens of hepatitis B virus (HBV) for packaging and transmission, but replicates its RNA in an HBV-independent fashion. HDV contains a 1.7-kb circular RNA genome that is folded into an unbranched rod-like structure via intramolecular base-pairing, and possesses ribozyme activity. The HDV genome does not encode an RNA-dependent RNA polymerase (RdRp), but is instead replicated by host RNA polymerase(s) via a rolling-circle mechanism. As such, HDV is similar to the viroid plant pathogens. Recent findings suggest that HDV can also undergo template-switching recombination, a well-documented process that has been found in a large number of RdRp-encoding RNA viruses and is thought to affect viral evolution and pathogenesis. This mini-review examines HDV RNA recombination and how it may improve our understanding of the capacities of host RNA polymerases beyond typical DNA-directed transcription, and speculates on the role of host RNA polymerase-directed RNA template-switching in the origin of HDV.
丁型肝炎病毒(HDV)需要乙型肝炎病毒(HBV)的表面抗原进行包装和传播,但其RNA以不依赖HBV的方式复制。HDV含有一个1.7kb的环状RNA基因组,该基因组通过分子内碱基配对折叠成无分支的棒状结构,并具有核酶活性。HDV基因组不编码RNA依赖性RNA聚合酶(RdRp),而是由宿主RNA聚合酶通过滚环机制进行复制。因此,HDV类似于类病毒植物病原体。最近的研究结果表明,HDV也可以进行模板转换重组,这是一个在大量编码RdRp的RNA病毒中都有记载的过程,被认为会影响病毒的进化和发病机制。这篇综述探讨了HDV RNA重组以及它如何增进我们对宿主RNA聚合酶能力的理解(超出了典型的DNA指导转录),并推测宿主RNA聚合酶指导的RNA模板转换在HDV起源中的作用。